Evidence map›Paper›PMID 24426864›Full record

ArticleHSS journal : the musculoskeletal journal of Hospital for Special Surgery2013

Use of imatinib in the prevention of heterotopic ossification.

Clément M L Werner, Stefan M Zimmermann, Carola C Würgler-Hauri, Joseph M Lane, Guido A Wanner, Hans-Peter Simmen

Open access · greenAbstract read
In one paragraph

Article in HSS journal : the musculoskeletal journal of Hospital for Special Surgery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP Signaling.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2016
    Article
  12. Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Clément M L WernerDepartment of Traumatology, University Hospital, Zurich, Switzerland ; Klinik für Unfallchirurgie, UniversitätsSpital Zürich, Rämistrasse 100, 8091 Zürich, Switzerland.
Stefan M ZimmermannDepartment of Traumatology, University Hospital, Zurich, Switzerland.
Carola C Würgler-HauriDepartment of Traumatology, University Hospital, Zurich, Switzerland.
Joseph M LaneHospital for Special Surgery, 535 East 70th Street, New York, NY 10021 USA.
Guido A WannerDepartment of Traumatology, University Hospital, Zurich, Switzerland.
Hans-Peter SimmenDepartment of Traumatology, University Hospital, Zurich, Switzerland.
University Hospital of Zurich · CHHospital for Special Surgery · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterotopic ossification (HO) is a common complication following orthopedic and trauma surgery, which may have substantial negative effects on the postoperative outcome. Angiogenesis appears to play a critical role in heterotopic ossification. One of the involved signaling molecules is platelet-derived growth factor (PDGF) which may be inhibited by imatinib. QUESTIONS/PURPOSES: Our goal was to prevent HO by pharmacologically interfering with the molecular signaling pathways involved in the developmental process. We hypothesized that by administering a proven inhibitor of PDGF expression, heterotopic bone formation may be prevented.

methodsThe effect of imatinib on HO formation was studied in a murine model which reliably produces islets of HO within the soft tissue following Achilles tenotomy. The control group underwent Achilles tenotomy only. The imatinib group received imatinib mesylate. After trial completion, the limbs were harvested and scanned by micro-CT. Heterotopic bone volume was then identified and quantified.

resultsThe mean volume of heterotopic bone formed in the control group was 0.976mm(3) compared to 0.221 mm(3) in the imatinib group. The volume of HO in the treatment group was reduced by 85% compared to the control group.

conclusionsThe administration of imatinib was associated with a significantly reduced volume of HO. This may be due to the inhibitory effect of imatinib on the PDGF signaling pathway during development of HO. CLINICAL RELEVANCE: The successful reduction of HO formation following imatinib administration has led to further insight concerning the pathogenesis of HO which in the future may lead to new clinical approaches towards the prevention of HO.

Indexed as

heterotopic ossificationimatinib mesylatemurinePDGFprevention

Identifiers

PMID24426864
PMCPMC3757489
OpenAlexW2032187587

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.